The transaction aims to enhance operational excellence, unlock additional growth opportunities, and further strengthen Samsung Biologics' position as a leading global multi-modality CDMO.
Explore practical approaches to sterility assurance, contamination control, GMP compliance, and advanced manufacturing considerations in this new eBook.
Sentry BioPharma Services ApS (Sentry EU) is a contract service organization (CSO) which supports the life science industry throughout the drug development life cycle by offering cGMP temperature-controlled storage, distribution, logistics, and EMA compliant labeling and packaging services. Sentry EU's Qualified Person (QP) facilitates import/export of pharmaceuticals to/from the EU via QP audits, QP-to-QP agreements, and batch certification/declarations. Sentry EU’s validated software, cGMP storage and drug distribution facility, industry expertise, and stringent quality standards support pharmaceutical supply chain integrity throughout manufacturing, packaging, storage and distribution.
QCL is a CDMO privately owned and operated since 1998. We excel in pre-formulation, formulation development, and delivering early phase clinical trial materials on aggressive timelines. We provide analytical development and validation, stability studies, and testing of small and large molecule APIs, finished products, and raw materials. New construction doubles our footprint to 200,000 sq. ft., expanding services into late phase clinical and small scale commercial GMP manufacturing including state of the art sterile fill-finish for both small and large molecules.
